TSMS Technical Project Manager

Your Role: TSMS Technical Project Manager The TSMS Technical Project Manager is responsible for coordinating cross-functional projects within the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility. This role ensures alignment with scientific, regulatory, and business objectives while managing timelines, resources, and project execution. Partnering closely with Manufacturing, Quality, Engineering, IT, and other functions, this position provides leadership and structure to successfully deliver technical and operational projects. Your Responsibilities: Develop and maintain detailed project plans, including scope, timelines, milestones, and resource allocation to ensure successful project delivery. Drive execution of cross-functional project plans, proactively identifying risks and developing mitigation and contingency strategies to ensure project success. Collaborate with internal teams, external partners, and vendors to achieve project objectives while maintaining alignment across all stakeholders. Communicate project status, risks, and key updates clearly and effectively to stakeholders and leadership. Partner with cross-functional teams to identify strategic and operational challenges that may impact project execution and develop solutions to address them. Act as a liaison between TS/MS, R&D, Operations, and other business functions, tailoring communication for both technical and non-technical audiences. Gather inputs and coordinate activities to develop and execute manufacturing project plans for development and commercial programs. What You Need to Succeed (minimum qualifications): Education: Bachelor’s or Master’s degree in Science, Engineering (Mechanical, Chemical), Pharmaceutical Technology, or a related field (or equivalent experience). Experience: 5+ years of experience in the pharmaceutical or biotech industry, including at least 2 years of project management experience. Top 2 Skills: Strong project management and organizational skills with the ability to manage timelines, resources, and risks; and the ability to collaborate cross-functionally and communicate effectively with both technical and non-technical stakeholders. Working knowledge of cGMP standards and regulatory requirements, with proficiency in project management tools such as MS Project, Excel, and PowerPoint. What will give you a competitive edge (preferred qualifications): PMP certification or equivalent project management training. Strong attention to detail with high personal standards for quality and ethics. Proven ability to build and maintain strong cross-functional relationships across all levels of the organization. Working knowledge of USDA, FDA, and EU GMP regulations for veterinary biologics. Additional Information: Location: Elwood, Kansas Elanco Benefits and Perks: We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include: Multiple relocation packages Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO) 8-week parental leave 9 Employee Resource Groups Annual bonus offering Up to 6% 401K matching Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #J-18808-Ljbffr Dormont Manufacturing Co